Variant DetailsVariant: esv3602721Internal ID | 6642977 | Landmark | | Location Information | | Cytoband | 4q31.3 | Allele length | Assembly | Allele length | hg38 | 2603 | hg19 | 2603 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv11655711, essv11655704, essv11655710, essv11655714, essv11655706, essv11655705, essv11655707, essv11655712, essv11655708, essv11655709, essv11655719, essv11655715, essv11655716, essv11655717, essv11655718, essv11655713 | Samples | HG02890, HG02583, NA20294, NA20359, NA20287, NA19923, HG03556, NA20340, NA19209, HG03058, NA19403, HG02577, NA19099, HG03433, HG02052, NA19129 | Known Genes | TRIM2 | Method | Sequencing | Analysis | | Platform | Multiple platforms | Comments | | Reference | 1000_Genomes_Consortium_Phase_3 | Pubmed ID | 21293372 | Accession Number(s) | esv3602721
| Frequency | Sample Size | 2504 | Observed Gain | 0 | Observed Loss | 16 | Observed Complex | 0 | Frequency | n/a |
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