Variant DetailsVariant: esv3637674 Internal ID | 6677776 | Landmark | | Location Information | | Cytoband | 16p13.3 | Allele length | Assembly | Allele length | hg38 | 1902 | hg19 | 1902 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv15363292, essv15363291, essv15363285, essv15363280, essv15363270, essv15363293, essv15363276, essv15363284, essv15363277, essv15363278, essv15363298, essv15363282, essv15363272, essv15363265, essv15363268, essv15363281, essv15363295, essv15363288, essv15363269, essv15363301, essv15363299, essv15363275, essv15363302, essv15363266, essv15363264, essv15363297, essv15363271, essv15363286, essv15363294, essv15363267, essv15363289, essv15363279, essv15363273, essv15363283, essv15363296, essv15363287, essv15363290, essv15363274, essv15363300 | Samples | HG03121, HG03548, NA19399, NA20298, HG02589, NA18870, NA19314, HG03095, HG03436, HG03385, NA19448, HG02325, HG03578, NA18868, NA19207, HG02420, NA18864, HG03114, NA19908, HG02334, NA18933, NA19184, HG02511, HG02554, NA19982, HG02450, HG02470, NA18907, HG02455, NA19380, HG03557, HG02814, HG03084, HG03063, HG03258, HG03410, HG02851, NA19431, HG03196 | Known Genes | TRAP1 | Method | Sequencing | Analysis | | Platform | Multiple platforms | Comments | | Reference | 1000_Genomes_Consortium_Phase_3 | Pubmed ID | 21293372 | Accession Number(s) | esv3637674
| Frequency | Sample Size | 2504 | Observed Gain | 0 | Observed Loss | 39 | Observed Complex | 0 | Frequency | n/a |
|
|