Variant DetailsVariant: dgv10347n54Internal ID | 20143771 | Landmark | | Location Information | | Cytoband | 6p21.33 | Allele length | Assembly | Allele length | hg38 | 69023 | hg19 | 69023 | hg18 | 69023 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nsv601277, nsv601262, nsv601284, nsv601278, nsv601329, nsv601261, nsv601263, nsv601298, nsv601258, nsv601330, nsv601257, nsv601357, nsv601339, nsv601260, nsv601300, nsv601299, nsv601259 | Samples | | Known Genes | HCG4B, HLA-A, 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) | dgv10347n54
| Frequency | Sample Size | 17421 | Observed Gain | 0 | Observed Loss | 42 | Observed Complex | 0 | Frequency | n/a |
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