| EX0355 CHROMULTRA CHROMOSOME SNP HD MICROARRAY |
| Specimen: |
4 mL (2 mL min.) whole blood in 1 Lavender top (EDTA) tube. Ship refrigerated. DO NOT FREEZE. |
| Stability: |
| Room |
Refrigerated |
Frozen |
| NA |
24 hrs |
NA |
|
| Method: |
Affymetrix CytoScan™ HD microarray |
| Comment: |
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| Report: |
Contact us to know the TAT. |
| Usage: |
SNP array is a high-resolution method for detecting copy number changes (gains or losses) across the entire genome in a single assay. This platform is also capable of detecting regions of homozygosity related to uniparental disomy or identity by descent. Indications for ordering include the following: Individuals with developmental delay/intellectual disability (with or without dysmorphic features), multiple congenital anomalies, autism spectrum disorder/pervasive developmental disorder, epilepsy/seizures, heart defects, family history of a chromosomal abnormality resulting in a genomic imbalance. This test is also able to further characterize certain chromosomal abnormalities including marker or ring chromosomes, Deletions or duplications, Unbalanced translocations, and Apparently balanced de-novo rearrangements in individuals with abnormal phenotypes. |
| Doctor Specialty: |
Pediatrician |
| Disease: |
Genetic disorders |
| Components: |
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| Courier Charges: |
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| Home Collection: |
Available (*T&C Apply) |
| Department: |
CYTOGENETICS |
| Pre Test Information: |
A duly filled Genomic Microarray Requisition Form is mandatory. |
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