Variant DetailsVariant: esv3643733Internal ID | 6683803 | Landmark | | Location Information | | Cytoband | 19p13.12 | Allele length | Assembly | Allele length | hg38 | 2902 | hg19 | 2902 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv15997194, essv15997196, essv15997195, essv15997193, essv15997192, essv15997191, essv15997189, essv15997190 | Samples | HG02890, HG02595, NA18864, HG03397, HG02586, HG02594, HG03279, NA20289 | Known Genes | IL27RA | Method | Sequencing | Analysis | | Platform | Multiple platforms | Comments | | Reference | 1000_Genomes_Consortium_Phase_3 | Pubmed ID | 21293372 | Accession Number(s) | esv3643733
| Frequency | Sample Size | 2504 | Observed Gain | 0 | Observed Loss | 8 | Observed Complex | 0 | Frequency | n/a |
|
|