Variant DetailsVariant: esv3627899Internal ID | 6668043 | Landmark | | Location Information | | Cytoband | 11q23.3 | Allele length | Assembly | Allele length | hg38 | 2112 | hg19 | 2112 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv14294707, essv14294704, essv14294702, essv14294703, essv14294706, essv14294710, essv14294709, essv14294708, essv14294705 | Samples | HG04212, HG03944, HG01676, HG02697, HG00239, HG01630, HG01777, NA20849, HG00581 | Known Genes | TRIM29 | Method | Sequencing | Analysis | | Platform | Multiple platforms | Comments | | Reference | 1000_Genomes_Consortium_Phase_3 | Pubmed ID | 21293372 | Accession Number(s) | esv3627899
| Frequency | Sample Size | 2504 | Observed Gain | 0 | Observed Loss | 9 | Observed Complex | 0 | Frequency | n/a |
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