Variant DetailsVariant: esv3624922 Internal ID | 6665084 | Landmark | | Location Information | | Cytoband | 10q26.3 | Allele length | Assembly | Allele length | hg38 | 946 | hg19 | 946 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv13973309, essv13973306, essv13973289, essv13973311, essv13973290, essv13973291, essv13973314, essv13973288, essv13973297, essv13973313, essv13973315, essv13973312, essv13973296, essv13973303, essv13973293, essv13973305, essv13973301, essv13973292, essv13973295, essv13973307, essv13973294, essv13973298, essv13973302, essv13973304, essv13973308, essv13973310, essv13973300, essv13973299 | Samples | NA18969, HG02069, NA18619, HG00369, HG00632, HG00309, HG00530, HG00268, HG00282, HG01864, HG00556, HG01845, HG00275, HG00404, HG00476, HG00336, NA18952, HG00353, HG00308, HG00319, HG02139, HG02188, HG00378, HG00656, NA18609, HG00180, HG02060, HG00581 | Known Genes | MGMT | Method | Sequencing | Analysis | | Platform | Multiple platforms | Comments | | Reference | 1000_Genomes_Consortium_Phase_3 | Pubmed ID | 21293372 | Accession Number(s) | esv3624922
| Frequency | Sample Size | 2504 | Observed Gain | 0 | Observed Loss | 28 | Observed Complex | 0 | Frequency | n/a |
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