Variant DetailsVariant: esv3637629Internal ID | 6677732 | Landmark | | Location Information | | Cytoband | 16p13.3 | Allele length | Assembly | Allele length | hg38 | 824 | hg19 | 824 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv15362424, essv15362418, essv15362419, essv15362422, essv15362425, essv15362421, essv15362427, essv15362420, essv15362417, essv15362426, essv15362423 | Samples | HG00384, HG00318, HG00364, HG00115, HG00341, HG00346, HG00369, HG00323, NA20515, HG01200, HG00186 | Known Genes | TRAF7 | Method | Sequencing | Analysis | | Platform | Multiple platforms | Comments | | Reference | 1000_Genomes_Consortium_Phase_3 | Pubmed ID | 21293372 | Accession Number(s) | esv3637629
| Frequency | Sample Size | 2504 | Observed Gain | 0 | Observed Loss | 11 | Observed Complex | 0 | Frequency | n/a |
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