Variant DetailsVariant: nsv524894Internal ID | 15105501 | Landmark | | Location Information | | Cytoband | 9q22.32 | Allele length | Assembly | Allele length | hg38 | 2815 | hg19 | 2815 | hg18 | 2815 | hg17 | 2815 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv700900 | Samples | | Known Genes | ERCC6L2, LINC00476 | Method | SNP array | Analysis | Sample-level CNVs | Platform | GPL6434 | Comments | | Reference | Shaikh_et_al_2009 | Pubmed ID | 19592680 | Accession Number(s) | nsv524894
| Frequency | Sample Size | 2026 | Observed Gain | 0 | Observed Loss | 1 | Observed Complex | 0 | Frequency | n/a |
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