Variant DetailsVariant: esv3638018Internal ID | 6678116 | Landmark | | Location Information | | Cytoband | 16p13.11 | Allele length | Assembly | Allele length | hg38 | 24196 | hg19 | 24196 |
| Variant Type | CNV gain | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | dgv482e214 | Supporting Variants | essv15385481, essv15385495, essv15385491, essv15385487, essv15385497, essv15385493, essv15385498, essv15385480, essv15385496, essv15385483, essv15385486, essv15385490, essv15385482, essv15385484, essv15385494, essv15385485, essv15385492, essv15385489, essv15385488 | Samples | NA21142, NA20786, NA21098, HG03294, HG01204, HG03199, HG01468, HG01375, HG01501, NA19256, NA21099, HG02888, NA21143, HG04161, HG00766, HG03518, HG03072, HG02219, NA18944 | Known Genes | PDXDC1 | Method | Sequencing | Analysis | | Platform | Multiple platforms | Comments | | Reference | 1000_Genomes_Consortium_Phase_3 | Pubmed ID | 21293372 | Accession Number(s) | esv3638018
| Frequency | Sample Size | 2504 | Observed Gain | 19 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
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