Variant DetailsVariant: esv3626656Internal ID | 6666806 | Landmark | | Location Information | | Cytoband | 11q13.1 | Allele length | Assembly | Allele length | hg38 | 929 | hg19 | 929 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv14184918, essv14184915, essv14184919, essv14184916, essv14184917, essv14184924, essv14184925, essv14184923, essv14184921, essv14184922, essv14184920, essv14184914 | Samples | HG03800, HG01795, HG02360, HG03805, HG03823, NA19000, NA18555, NA18536, NA18615, NA19078, HG00513, HG01912 | Known Genes | MACROD1 | Method | Sequencing | Analysis | | Platform | Multiple platforms | Comments | | Reference | 1000_Genomes_Consortium_Phase_3 | Pubmed ID | 21293372 | Accession Number(s) | esv3626656
| Frequency | Sample Size | 2504 | Observed Gain | 0 | Observed Loss | 12 | Observed Complex | 0 | Frequency | n/a |
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