Variant DetailsVariant: esv2665628Internal ID | 9585047 | Landmark | | Location Information | | Cytoband | 16p13.3 | Allele length | Assembly | Allele length | hg38 | 655 | hg19 | 655 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv5555377, essv5416712, essv5708832, essv6458604, essv6562547, essv5845594, essv5771473, essv6326738 | Samples | NA19819, NA20808, NA19404, NA19471, NA19391, NA19338, NA19398, NA19248 | Known Genes | LUC7L | Method | Merging | Analysis | No reference, merging analysis | Platform | Merging | Comments | | Reference | 1000_Genomes_Consortium_Phase_1 | Pubmed ID | 23128226 | Accession Number(s) | esv2665628
| Frequency | Sample Size | 1151 | Observed Gain | 0 | Observed Loss | 8 | Observed Complex | 0 | Frequency | n/a |
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