Variant DetailsVariant: dgv6942n100Internal ID | 20158558 | Landmark | | Location Information | | Cytoband | 8p23.1 | Allele length | Assembly | Allele length | hg38 | 112534 | hg19 | 112534 | hg18 | 112534 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nsv1029433, nsv1028014, nsv1026197, nsv1030754, nsv1026807, nsv1034263, nsv1026462, nsv1019456, nsv1024826, nsv1024244, nsv1031168, nsv1016110, nsv1029791, nsv1028275, nsv1023627, nsv1035114, nsv1033679 | Samples | | Known Genes | DEFB104A, DEFB104B, DEFB105A, DEFB105B, DEFB106A, DEFB106B, DEFB107A, DEFB107B, PRR23D1, PRR23D2, SPAG11B | 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) | dgv6942n100
| Frequency | Sample Size | 29084 | Observed Gain | 0 | Observed Loss | 24 | Observed Complex | 0 | Frequency | n/a |
|
|