{"product_id":"chromosomal-microarraycma315k-affymetrix-cytoscan-optima-and-couple-karyotyping-combo","title":"Chromosomal Microarray(CMA315k) -Affymetrix Cytoscan Optima and Couple Karyotyping Combo","description":"\u003cp\u003eAmniotic Fluid\/ Chorionic Villus Sample\/Peripheral Venous Blood\/Cord blood,\/Extracted DNA\/Dry Blood Spot\u003c\/p\u003e\n\u003cdiv class=\"qMYqUG_convSearchResultHighlightRoot\"\u003e\n\u003cdiv class=\"\" data-turn-id-container=\"request-WEB:e1c0cdac-87bf-431a-be7e-9a43962869d7-5\" data-is-intersecting=\"true\"\u003e\n\u003csection class=\"text-token-text-primary w-full focus:outline-none has-data-writing-block:pointer-events-none [\u0026amp;:has([data-writing-block])\u0026gt;*]:pointer-events-auto R6Vx5W_threadScrollVars scroll-mb-[calc(var(--scroll-root-safe-area-inset-bottom,0px)+var(--thread-response-height))] scroll-mt-[calc(var(--header-height)+min(200px,max(70px,20svh)))]\" dir=\"auto\" data-turn-id=\"request-WEB:e1c0cdac-87bf-431a-be7e-9a43962869d7-5\" data-turn-id-container=\"request-WEB:e1c0cdac-87bf-431a-be7e-9a43962869d7-5\" data-testid=\"conversation-turn-2\" data-scroll-anchor=\"false\" data-turn=\"assistant\"\u003e\n\u003cdiv class=\"text-base my-auto mx-auto pb-10 [--thread-content-margin:var(--thread-content-margin-xs,calc(var(--spacing)*4))] @w-sm\/main:[--thread-content-margin:var(--thread-content-margin-sm,calc(var(--spacing)*6))] @w-lg\/main:[--thread-content-margin:var(--thread-content-margin-lg,calc(var(--spacing)*16))] px-(--thread-content-margin)\"\u003e\n\u003cdiv data-conversation-screenshot-content=\"\" class=\"[--thread-content-max-width:40rem] @w-lg\/main:[--thread-content-max-width:48rem] mx-auto max-w-(--thread-content-max-width) flex-1 group\/turn-messages focus-visible:outline-hidden relative flex w-full min-w-0 flex-col agent-turn\"\u003e\n\u003cdiv class=\"flex max-w-full flex-col gap-4 grow\"\u003e\n\u003cdiv data-message-author-role=\"assistant\" data-message-id=\"ee9e325d-8673-4e14-ab2f-359452f39547\" data-turn-start-message=\"true\" dir=\"auto\" data-message-model-slug=\"gpt-5-5\" class=\"min-h-8 text-message relative flex w-full flex-col items-end gap-2 text-start break-words whitespace-normal outline-none keyboard-focused:focus-ring [.text-message+\u0026amp;]:mt-1\" tabindex=\"0\"\u003e\n\u003cdiv class=\"flex w-full flex-col gap-1 empty:hidden\"\u003e\n\u003cdiv class=\"markdown prose dark:prose-invert wrap-break-word w-full light markdown-new-styling\"\u003e\n\u003ch3 data-section-id=\"1q0t1ya\" data-start=\"0\" data-end=\"93\"\u003eChromosomal Microarray (CMA 315K) – Affymetrix CytoScan Optima \u0026amp; Couple Karyotyping Combo\u003c\/h3\u003e\n\u003cp data-start=\"95\" data-end=\"112\"\u003e\u003cstrong data-start=\"95\" data-end=\"112\"\u003eTest Overview\u003c\/strong\u003e\u003c\/p\u003e\n\u003cp data-start=\"114\" data-end=\"775\"\u003eThe \u003cstrong data-start=\"118\" data-end=\"213\"\u003eChromosomal Microarray (CMA 315K) – Affymetrix CytoScan Optima and Couple Karyotyping Combo\u003c\/strong\u003e is a comprehensive genetic screening package designed to evaluate chromosomal abnormalities in both partners. It combines high-resolution chromosomal microarray analysis with conventional karyotyping to identify genetic variations that may affect fertility, pregnancy outcomes, recurrent miscarriages, congenital anomalies, or inherited chromosomal disorders. CMA provides detailed detection of microdeletions and microduplications, while karyotyping identifies large chromosomal rearrangements and balanced translocations. \u003cspan class=\"\" data-state=\"closed\"\u003e\u003c\/span\u003e\u003c\/p\u003e\n\u003ch3 data-section-id=\"1k1dw32\" data-start=\"777\" data-end=\"815\"\u003eWhat Does This Combo Test Include?\u003c\/h3\u003e\n\u003ch4 data-start=\"817\" data-end=\"858\"\u003e1. Chromosomal Microarray (CMA 315K)\u003c\/h4\u003e\n\u003cul data-start=\"859\" data-end=\"1256\"\u003e\n\u003cli data-section-id=\"1lm9y2m\" data-start=\"859\" data-end=\"914\"\u003eUses \u003cstrong data-start=\"866\" data-end=\"902\"\u003eAffymetrix CytoScan Optima Array\u003c\/strong\u003e technology.\u003c\/li\u003e\n\u003cli data-section-id=\"15ulgux\" data-start=\"915\" data-end=\"990\"\u003eAnalyzes over \u003cstrong data-start=\"931\" data-end=\"962\"\u003e315,000 chromosomal markers\u003c\/strong\u003e for genome-wide assessment.\u003c\/li\u003e\n\u003cli data-section-id=\"1ccxwia\" data-start=\"991\" data-end=\"1256\"\u003eDetects:\n\u003cul data-start=\"1004\" data-end=\"1256\"\u003e\n\u003cli data-section-id=\"3nzhfx\" data-start=\"1004\" data-end=\"1042\"\u003eMicrodeletions and microduplications\u003c\/li\u003e\n\u003cli data-section-id=\"66m5d1\" data-start=\"1045\" data-end=\"1076\"\u003eCopy Number Variations (CNVs)\u003c\/li\u003e\n\u003cli data-section-id=\"yw6urr\" data-start=\"1079\" data-end=\"1124\"\u003eAneuploidies (extra or missing chromosomes)\u003c\/li\u003e\n\u003cli data-section-id=\"8tbl7r\" data-start=\"1127\" data-end=\"1158\"\u003eRegions of homozygosity (ROH)\u003c\/li\u003e\n\u003cli data-section-id=\"1n8aqcu\" data-start=\"1161\" data-end=\"1187\"\u003eUniparental Disomy (UPD)\u003c\/li\u003e\n\u003cli data-section-id=\"g37h6a\" data-start=\"1190\" data-end=\"1256\"\u003eCertain forms of mosaicism \u003cspan class=\"\" data-state=\"closed\"\u003e\u003c\/span\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch4 data-start=\"1258\" data-end=\"1284\"\u003e2. Couple Karyotyping\u003c\/h4\u003e\n\u003cul data-start=\"1285\" data-end=\"1581\"\u003e\n\u003cli data-section-id=\"188x383\" data-start=\"1285\" data-end=\"1353\"\u003eExamines the number and structure of chromosomes in both partners.\u003c\/li\u003e\n\u003cli data-section-id=\"tq4utv\" data-start=\"1354\" data-end=\"1581\"\u003eDetects:\n\u003cul data-start=\"1367\" data-end=\"1581\"\u003e\n\u003cli data-section-id=\"1j81m3w\" data-start=\"1367\" data-end=\"1407\"\u003eBalanced and unbalanced translocations\u003c\/li\u003e\n\u003cli data-section-id=\"16b656u\" data-start=\"1410\" data-end=\"1422\"\u003eInversions\u003c\/li\u003e\n\u003cli data-section-id=\"ufw84u\" data-start=\"1425\" data-end=\"1470\"\u003eLarge chromosomal deletions or duplications\u003c\/li\u003e\n\u003cli data-section-id=\"p0uz1t\" data-start=\"1473\" data-end=\"1581\"\u003eNumerical chromosomal abnormalities such as trisomies and monosomies \u003cspan class=\"\" data-state=\"closed\"\u003e\u003c\/span\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3 data-section-id=\"168hjsr\" data-start=\"1583\" data-end=\"1617\"\u003eWho Should Consider This Test?\u003c\/h3\u003e\n\u003cul data-start=\"1619\" data-end=\"1976\"\u003e\n\u003cli data-section-id=\"1n79anf\" data-start=\"1619\" data-end=\"1656\"\u003eCouples with recurrent miscarriages\u003c\/li\u003e\n\u003cli data-section-id=\"1c0xxw6\" data-start=\"1657\" data-end=\"1686\"\u003eInfertility or subfertility\u003c\/li\u003e\n\u003cli data-section-id=\"1j1m82y\" data-start=\"1687\" data-end=\"1747\"\u003ePrevious child with genetic abnormalities or birth defects\u003c\/li\u003e\n\u003cli data-section-id=\"1xhsrvi\" data-start=\"1748\" data-end=\"1789\"\u003eFamily history of chromosomal disorders\u003c\/li\u003e\n\u003cli data-section-id=\"1ycyezv\" data-start=\"1790\" data-end=\"1818\"\u003eRepeated IVF\/ICSI failures\u003c\/li\u003e\n\u003cli data-section-id=\"e42iq4\" data-start=\"1819\" data-end=\"1883\"\u003eCouples planning pregnancy and seeking genetic risk assessment\u003c\/li\u003e\n\u003cli data-section-id=\"es73s1\" data-start=\"1884\" data-end=\"1976\"\u003eIndividuals with suspected chromosomal abnormalities \u003cspan class=\"\" data-state=\"closed\"\u003e\u003c\/span\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3 data-section-id=\"ycgkk5\" data-start=\"1978\" data-end=\"1994\"\u003eKey Benefits\u003c\/h3\u003e\n\u003cp data-start=\"1996\" data-end=\"2427\"\u003e✔ Comprehensive evaluation of chromosomal health in both partners\u003cbr data-start=\"2061\" data-end=\"2064\"\u003e✔ Detects abnormalities not visible through routine genetic testing\u003cbr data-start=\"2131\" data-end=\"2134\"\u003e✔ Helps identify causes of infertility and recurrent pregnancy loss\u003cbr data-start=\"2201\" data-end=\"2204\"\u003e✔ Assists in reproductive planning and genetic counseling\u003cbr data-start=\"2261\" data-end=\"2264\"\u003e✔ Supports informed IVF and prenatal testing decisions\u003cbr data-start=\"2318\" data-end=\"2321\"\u003e✔ Higher diagnostic yield when CMA and karyotyping are used together \u003cspan class=\"\" data-state=\"closed\"\u003e\u003c\/span\u003e\u003c\/p\u003e\n\u003ch3 data-section-id=\"e3hbz\" data-start=\"2429\" data-end=\"2451\"\u003eSample Requirement\u003c\/h3\u003e\n\u003cul data-start=\"2453\" data-end=\"2547\"\u003e\n\u003cli data-section-id=\"11vyhxt\" data-start=\"2453\" data-end=\"2547\"\u003e\n\u003cstrong data-start=\"2455\" data-end=\"2483\"\u003ePeripheral Blood (EDTA):\u003c\/strong\u003e 3–5 mL from each partner. \u003cspan class=\"\" data-state=\"closed\"\u003e\u003c\/span\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3 data-section-id=\"1sm13zx\" data-start=\"2549\" data-end=\"2567\"\u003eReporting Time\u003c\/h3\u003e\n\u003cul data-start=\"2569\" data-end=\"2681\"\u003e\n\u003cli data-section-id=\"1f5zpzo\" data-start=\"2569\" data-end=\"2681\"\u003eApproximately \u003cstrong data-start=\"2585\" data-end=\"2607\"\u003e10–21 working days\u003c\/strong\u003e, depending on laboratory protocols. \u003cspan class=\"\" data-state=\"closed\"\u003e\u003c\/span\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3 data-section-id=\"16153u4\" data-start=\"2683\" data-end=\"2701\"\u003eInterpretation\u003c\/h3\u003e\n\u003cp data-start=\"2703\" data-end=\"3034\"\u003eA normal result reduces the likelihood of significant chromosomal abnormalities, while an abnormal result may identify genetic changes associated with infertility, recurrent pregnancy loss, developmental disorders, or inherited chromosomal conditions. Genetic counseling is recommended for interpretation and reproductive planning.\u003c\/p\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003cdiv class=\"z-0 flex min-h-[46px] justify-start\"\u003e\u003cbr\u003e\u003c\/div\u003e\n\u003cdiv class=\"mt-3 w-full empty:hidden\"\u003e\n\u003cdiv class=\"text-center\"\u003e\u003cbr\u003e\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/section\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e","brand":"Lifecell Diagnostics","offers":[{"title":"Default Title","offer_id":44007227293831,"sku":null,"price":11935.0,"currency_code":"INR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0691\/4241\/3447\/files\/7d14ae6b-9dd9-4b33-835c-bff897ec1cca.png?v=1780566934","url":"https:\/\/ourdermastore.com\/products\/chromosomal-microarraycma315k-affymetrix-cytoscan-optima-and-couple-karyotyping-combo","provider":"Ourdermastore ","version":"1.0","type":"link"}