Variant DetailsVariant: dgv2514n100Internal ID | 20154130 | Landmark | | Location Information | | Cytoband | 15q13.2 | Allele length | Assembly | Allele length | hg38 | 363611 | hg19 | 363611 | hg18 | 363611 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nsv1054586, nsv1042386, nsv1043559, nsv1049177, nsv1051871, nsv1040351, nsv1053900, nsv1054935, nsv1047012, nsv1051737 | Samples | | Known Genes | ARHGAP11B, CHRFAM7A, GOLGA8H, 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) | dgv2514n100
| Frequency | Sample Size | 29084 | Observed Gain | 0 | Observed Loss | 18 | Observed Complex | 0 | Frequency | n/a |
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