- PID
- 3696957
Chromosomal Microarray Test CMA
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Chromosomal Microarray Test(CMA)
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Product Summary
EDGC CMA utilizes Illumina 'sGlobal Screening Array (GSA) to identify clinically relevant micro deletions/ duplication and CNVs.
Detailed Description
┃Benefits┃
- CMA helps to identify diseases in approximately 15-20% of individuals with unexplained developmental delay, autism spectrum disorder and multiple congenital anomalies
- Validated on 5,399 clinical samples
- Identifies CNVs and copy neutral changes (i.e., uniparental disomy)
- Evaluates 750K markers
┃Test Details┃
Specimen: Blood, gDNA, amniotic fluid
TAT: 10-14 days
Test Method : SNP array
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