Variant DetailsVariant: dgv2563n100![](http://dgv.tcag.ca/gb2/gbrowse_img/dgv2_hg18/?name=chr15:32501403..32665045;width=800;overview=1) Internal ID | 20154179 | Landmark | | Location Information | | Cytoband | 15q14 | Allele length | Assembly | Allele length | hg38 | 163643 | hg19 | 163643 | hg18 | 163643 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nsv1053800, nsv1048580, nsv1046979, nsv1048956, nsv1047637, nsv1043642, nsv1051213, nsv1049914, nsv1053356, nsv1040772, nsv1045068, nsv1035639, nsv1054994, nsv1039342, nsv1053795, nsv1040470, nsv1043665, nsv1045531, nsv1054359, nsv1038550, nsv1050147, nsv1038804, nsv1039545, nsv1053349, nsv1040243, nsv1046335, nsv1046704, nsv1041494, nsv1053703, nsv1041114, nsv1041232, nsv1044586, nsv1041760, nsv1037332, nsv1042456, nsv1046848 | Samples | | Known Genes | GOLGA8A, GOLGA8B, MIR1233-1, MIR1233-2 | 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) | dgv2563n100
| Frequency | Sample Size | 29084 | Observed Gain | 0 | Observed Loss | 201 | Observed Complex | 0 | Frequency | n/a |
|
|