Variant DetailsVariant: essv6989285Internal ID | 12627772 | Landmark | | Location Information | | Cytoband | 15q13.1 | Allele length | Assembly | Allele length | hg38 | 1301591 | hg19 | 1348648 | hg18 | 1336899 | hg17 | 1336899 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | S | Merged Variants | esv2751526 | Supporting Variants | | Samples | BEC_521 | Known Genes | APBA2, FAM189A1, GOLGA6L7P, LOC100289656, LOC646278, NDNL2, TJP1, WHAMMP2 | Method | SNP array | Analysis | | Platform | Affymetrix Mapping 250K Nsp SNP Array | Comments | | Reference | Pinto_et_al_2007 | Pubmed ID | 17911159 | Accession Number(s) | essv6989285
| Frequency | Sample Size | 771 | Observed Gain | 0 | Observed Loss | 1 | Observed Complex | 0 | Frequency | n/a |
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