Variant DetailsVariant: dgv3669n100Internal ID | 20155285 | Landmark | | Location Information | | Cytoband | 19q13.42 | Allele length | Assembly | Allele length | hg38 | 85990 | hg19 | 85978 | hg18 | 85978 |
| Variant Type | CNV gain | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nsv1059091, nsv1061438, nsv1061067, nsv1055171, nsv1064985, nsv1064780, nsv1064703 | Samples | | Known Genes | KIR2DL1, KIR2DL3, KIR2DL4, KIR3DL1, KIR3DL3, LOC100287534 | 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) | dgv3669n100
| Frequency | Sample Size | 29084 | Observed Gain | 22 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
|
|