Variant DetailsVariant: esv3611659Internal ID | 6651877 | Landmark | | Location Information | | Cytoband | 6q27 | Allele length | Assembly | Allele length | hg38 | 34918 | hg19 | 34918 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv12643448, essv12643444, essv12643445, essv12643447, essv12643446, essv12643449, essv12643443 | Samples | HG02890, HG03241, HG03460, HG02571, HG03428, HG03279, HG03401 | Known Genes | TTLL2 | Method | Sequencing | Analysis | | Platform | Multiple platforms | Comments | | Reference | 1000_Genomes_Consortium_Phase_3 | Pubmed ID | 21293372 | Accession Number(s) | esv3611659
| Frequency | Sample Size | 2504 | Observed Gain | 0 | Observed Loss | 7 | Observed Complex | 0 | Frequency | n/a |
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