| Variant DetailsVariant: dgv6565n54| Internal ID | 20139989 |  | Landmark |  |  | Location Information |  |  | Cytoband | 19q13.42 |  | Allele length | | Assembly | Allele length |  | hg38 | 13183 |  | hg19 | 13183 |  | hg18 | 13183 | 
 |  | Variant Type | CNV loss |  | Copy Number |  |  | Allele State |  |  | Allele Origin |  |  | Probe Count |  |  | Validation Flag |  |  | Merged Status | M |  | Merged Variants |  |  | Supporting Variants | nsv580259, nsv580254 |  | Samples |  |  | Known Genes | KIR2DL3 |  | Method | SNP array |  | Analysis | Illumina SNP array copy number analysis |  | Platform | Not reported |  | Comments |  |  | Reference | Cooper_et_al_2011 |  | Pubmed ID | 21841781 |  | Accession Number(s) | dgv6565n54 
 |  | Frequency | | Sample Size | 17421 |  | Observed Gain | 0 |  | Observed Loss | 12 |  | Observed Complex | 0 |  | Frequency | n/a | 
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