Variant DetailsVariant: esv3626609Internal ID | 6666759 | Landmark | | Location Information | | Cytoband | 11q12.3 | Allele length | Assembly | Allele length | hg38 | 1409 | hg19 | 1409 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv14179715, essv14179716, essv14179712, essv14179709, essv14179706, essv14179714, essv14179704, essv14179703, essv14179718, essv14179710, essv14179711, essv14179713, essv14179708, essv14179717, essv14179707, essv14179705 | Samples | NA19020, NA18504, NA19107, NA19198, NA19347, HG02511, NA18915, HG03159, HG03202, HG02309, NA19376, HG02971, NA19102, HG02855, NA18511, HG03265 | Known Genes | AHNAK | Method | Sequencing | Analysis | | Platform | Multiple platforms | Comments | | Reference | 1000_Genomes_Consortium_Phase_3 | Pubmed ID | 21293372 | Accession Number(s) | esv3626609
| Frequency | Sample Size | 2504 | Observed Gain | 0 | Observed Loss | 16 | Observed Complex | 0 | Frequency | n/a |
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