Variant DetailsVariant: esv2664671 Internal ID | 9584090 | Landmark | | Location Information | | Cytoband | 6q27 | Allele length | Assembly | Allele length | hg38 | 1406 | hg19 | 1406 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv5726303, essv5564092, essv6190426, essv5396037, essv5531221, essv5583475, essv5942771, essv5427066, essv6510683, essv5966119, essv5843847, essv5515399, essv5420804, essv6271829, essv5622476, essv5572274, essv5660595, essv5924432, essv5443040, essv6418129, essv5768062, essv6214148, essv5935602, essv6389221, essv6208984 | Samples | NA19909, NA19350, NA18486, NA19393, NA19920, NA18916, NA18498, NA19404, NA18874, NA19445, NA18908, NA19247, NA19657, NA19437, NA19236, NA19982, NA18910, NA18907, NA19114, NA19453, NA19467, NA19223, NA19116, NA19129, NA19429 | Known Genes | CCR6 | Method | Merging | Analysis | No reference, merging analysis | Platform | Merging | Comments | High quality site | Reference | 1000_Genomes_Consortium_Phase_1 | Pubmed ID | 23128226 | Accession Number(s) | esv2664671
| Frequency | Sample Size | 1151 | Observed Gain | 0 | Observed Loss | 25 | Observed Complex | 0 | Frequency | n/a |
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