Variant DetailsVariant: nsv601241Internal ID | 16041964 | Landmark | | Location Information | | Cytoband | 6p21.33 | Allele length | Assembly | Allele length | hg38 | 35444 | hg19 | 35444 | hg18 | 35444 |
| Variant Type | CNV gain | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv1051733, nssv1154040, nssv1154039, nssv1051732 | Samples | HGDP00058, HGDP00098 | Known Genes | HLA-H | 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) | nsv601241
| Frequency | Sample Size | 17421 | Observed Gain | 4 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
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