Variant DetailsVariant: nsv527607Internal ID | 15108214 | Landmark | | Location Information | | Cytoband | 15q22.2 | Allele length | Assembly | Allele length | hg38 | 53305 | hg19 | 53305 | hg18 | 53305 | hg17 | 53305 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv704069 | Samples | | Known Genes | NARG2, RORA | Method | SNP array | Analysis | Sample-level CNVs | Platform | GPL6434 | Comments | | Reference | Shaikh_et_al_2009 | Pubmed ID | 19592680 | Accession Number(s) | nsv527607
| Frequency | Sample Size | 2026 | Observed Gain | 0 | Observed Loss | 1 | Observed Complex | 0 | Frequency | n/a |
|
|