Variant DetailsVariant: esv2672373 Internal ID | 9591792 | Landmark | | Location Information | | Cytoband | 14q32.32 | Allele length | Assembly | Allele length | hg38 | 741 | hg19 | 741 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv5713509, essv6500608, essv6494424, essv5430557, essv6370708, essv6457772, essv5507800, essv5587789, essv5788900, essv5666952, essv6249754, essv5403865, essv6588863, essv5447877, essv5784123, essv5950889, essv5989464, essv6578768, essv6372494, essv5861954, essv5983282, essv6351173, essv5904306, essv6063865, essv5979621 | Samples | NA19394, NA18502, NA19359, NA19819, NA20356, NA19448, NA19313, NA20287, NA19404, NA18908, NA19437, NA19982, NA20126, NA18910, NA19834, NA19256, NA19147, NA19439, NA19428, NA19311, HG01108, HG00259, NA19223, NA20289, NA19129 | Known Genes | TRAF3 | Method | Merging | Analysis | No reference, merging analysis | Platform | Merging | Comments | | Reference | 1000_Genomes_Consortium_Phase_1 | Pubmed ID | 23128226 | Accession Number(s) | esv2672373
| Frequency | Sample Size | 1151 | Observed Gain | 0 | Observed Loss | 25 | Observed Complex | 0 | Frequency | n/a |
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