Variant DetailsVariant: nssv692148Internal ID | 15082114 | Landmark | | Location Information | | Cytoband | 19q13.42 | Allele length | Assembly | Allele length | hg38 | 75023 | hg19 | 75026 | hg18 | 75026 | hg17 | 75026 |
| Variant Type | CNV loss | Copy Number | | Allele State | Heterozygous | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | S | Merged Variants | nsv517143 | Supporting Variants | | Samples | | Known Genes | KIR2DL4, KIR2DS4, KIR3DL1, KIR3DL2, LOC100287534 | Method | SNP array | Analysis | Sample-level CNVs | Platform | GPL6434 | Comments | | Reference | Shaikh_et_al_2009 | Pubmed ID | 19592680 | Accession Number(s) | nssv692148
| Frequency | Sample Size | 2026 | Observed Gain | 0 | Observed Loss | 1 | Observed Complex | 0 | Frequency | n/a |
|
|