CHROMULTRA CHROMOSOME SNP HD MICROARRAY
SNPÂ 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.
Parameter(s) covered : 1
Report Frequency: Sample Daily by 4 pm; Report 15 Working days
Special Instruction: Duly filled Genomic Microarray Requisition Form (Form 19) is mandatory.
Price : ₹ 27000.00
Parameters
- ChromUltra Chromosome SNP HD microarray