Variant DetailsVariant: esv2671960Internal ID | 9591379 | Landmark | | Location Information | | Cytoband | 6p21.1 | Allele length | Assembly | Allele length | hg38 | 438 | hg19 | 438 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv6478198, essv5790222, essv5426494, essv5513935, essv6016793, essv6044252 | Samples | NA19448, NA19385, NA19453, NA19436, NA19401, NA19434 | Known Genes | CUL9 | Method | Merging | Analysis | No reference, merging analysis | Platform | Merging | Comments | | Reference | 1000_Genomes_Consortium_Phase_1 | Pubmed ID | 23128226 | Accession Number(s) | esv2671960
| Frequency | Sample Size | 1151 | Observed Gain | 0 | Observed Loss | 6 | Observed Complex | 0 | Frequency | n/a |
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