Variant DetailsVariant: dgv2517n100Internal ID | 20154133 | Landmark | | Location Information | | Cytoband | 15q13.2 | Allele length | Assembly | Allele length | hg38 | 375475 | hg19 | 375475 | hg18 | 375475 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nsv1036312, nsv1044912, nsv1045010, nsv1052176 | Samples | | Known Genes | ARHGAP11B, CHRFAM7A, GOLGA8H, LOC100288637, LOC101059918, ULK4P1, ULK4P2 | 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) | dgv2517n100
| Frequency | Sample Size | 29084 | Observed Gain | 0 | Observed Loss | 6 | Observed Complex | 0 | Frequency | n/a |
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