Variant DetailsVariant: esv2663135 Internal ID | 9582554 | Landmark | | Location Information | | Cytoband | 3p26.3 | Allele length | Assembly | Allele length | hg38 | 206 | hg19 | 206 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv6328634, essv6133325, essv5681057, essv6181677, essv6246957, essv5999643, essv5611207, essv6433626, essv6340568, essv5422195, essv6272039, essv6207232, essv5842294, essv6132426, essv5807843, essv6331186, essv6461255, essv6218027, essv6220047, essv6568506, essv6012747, essv6415106, essv6352854 | Samples | NA18861, NA18486, NA20332, NA19377, NA19190, NA19920, NA18519, NA18489, NA19197, NA19189, NA18908, NA18871, NA20344, NA19461, NA18858, NA19436, NA19390, NA18517, NA19311, NA19360, NA19713, NA18873, NA18488 | Known Genes | CHL1 | Method | Merging | Analysis | No reference, merging analysis | Platform | Merging | Comments | | Reference | 1000_Genomes_Consortium_Phase_1 | Pubmed ID | 23128226 | Accession Number(s) | esv2663135
| Frequency | Sample Size | 1151 | Observed Gain | 0 | Observed Loss | 23 | Observed Complex | 0 | Frequency | n/a |
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