Variant DetailsVariant: esv3623859Internal ID | 6664026 | Landmark | | Location Information | | Cytoband | 10q22.3 | Allele length | Assembly | Allele length | hg38 | 1337 | hg19 | 1337 |
| Variant Type | OTHER inversion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv13864460, essv13864471, essv13864475, essv13864473, essv13864463, essv13864466, essv13864468, essv13864469, essv13864462, essv13864464, essv13864465, essv13864458, essv13864472, essv13864461, essv13864474, essv13864467, essv13864470, essv13864459 | Samples | NA19222, HG02337, NA20359, HG02595, HG03079, HG03352, NA18520, NA20342, HG03343, HG02678, HG03446, HG02983, NA19144, NA20362, HG03304, NA19223, HG03538, NA19153 | Known Genes | C10orf11 | Method | Sequencing | Analysis | | Platform | Multiple platforms | Comments | | Reference | 1000_Genomes_Consortium_Phase_3 | Pubmed ID | 21293372 | Accession Number(s) | esv3623859
| Frequency | Sample Size | 2504 | Observed Gain | 0 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
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