Variant DetailsVariant: dgv1098e199Internal ID | 20124400 | Landmark | | Location Information | | Cytoband | 6p21.33 | Allele length | Assembly | Allele length | hg38 | 104313 | hg19 | 104313 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | esv2673424, esv2674583 | Samples | HG01462, HG01140, NA19079, HG00740, NA20276 | Known Genes | HCG26, HCP5, MICA | Method | Merging | Analysis | No reference, merging analysis | Platform | Merging | Comments | | Reference | 1000_Genomes_Consortium_Phase_1 | Pubmed ID | 23128226 | Accession Number(s) | dgv1098e199
| Frequency | Sample Size | 1151 | Observed Gain | 0 | Observed Loss | 5 | Observed Complex | 0 | Frequency | n/a |
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