No.4 Niloo St., Valiasr Ave., Tehran, Iran · +98 21 8865 8752 · genpeima.com
Detect microdeletions, duplications, and copy number variations with unprecedented accuracy — plus homozygosity mapping that standard karyotyping simply can't provide.
Request a TestWhy SNP Array outperforms standard karyotyping for detecting genomic imbalance.
Detects very small chromosomal copy number variations (CNVs) invisible to standard karyotyping.
Identifies regions of homozygosity, critical for consanguineous families and recessive disease diagnosis.
Combines SNP and copy-number probes to maximize accuracy and eliminate false positives.
Amniotic fluid or CVS, for pregnancies with increased NT, structural anomalies, or high-risk NIPT results.
Peripheral blood, for developmental delay, intellectual disability, autism, or congenital anomalies.
Tumor profiling — somatic copy number alterations and loss of heterozygosity for translational research.
| Platform | Illumina Global Screening Array v3 (GSA v3), Illumina iScan™ |
|---|---|
| Total Markers | > 654,000 |
| Call Rate | > 99.8% |
| Reference Genome | GRCh37 / GRCh38 |
Talk to our team about ordering high-resolution SNP Array analysis for your patients or practice.
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