Variant DetailsVariant: dgv2495n100Internal ID | 20154111 | Landmark | | Location Information | | Cytoband | 15q13.2 | Allele length | Assembly | Allele length | hg38 | 566372 | hg19 | 566372 | hg18 | 566372 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nsv1042426, nsv1044368, nsv1039789, nsv1050658, nsv1040604 | Samples | | Known Genes | ARHGAP11B, CHRFAM7A, DKFZP434L187, GOLGA8H, GOLGA8J, GOLGA8T, LOC101059918, ULK4P1, ULK4P2, ULK4P3 | Method | SNP array | Analysis | Affymetrix SNP array copy number analysis | Platform | Affymetrix SNP Array 6.0 | Comments | | Reference | Coe_et_al_2014 | Pubmed ID | 25217958 | Accession Number(s) | dgv2495n100
| Frequency | Sample Size | 29084 | Observed Gain | 0 | Observed Loss | 5 | Observed Complex | 0 | Frequency | n/a |
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