Variant DetailsVariant: esv3588025| Internal ID | 6975449 | | Landmark | | | Location Information | | | Cytoband | 1q25.2 | | Allele length | | Assembly | Allele length | | hg38 | 5362 | | hg19 | 5362 |
| | Variant Type | CNV loss | | Copy Number | | | Allele State | | | Allele Origin | | | Probe Count | | | Validation Flag | | | Merged Status | M | | Merged Variants | dgv63e214 | | Supporting Variants | essv10193415, essv10193414 | | Samples | HG02819, NA19716 | | Known Genes | | | Method | Sequencing | | Analysis | | | Platform | Multiple platforms | | Comments | | | Reference | 1000_Genomes_Consortium_Phase_3 | | Pubmed ID | 21293372 | | Accession Number(s) | esv3588025
| | Frequency | | Sample Size | 2504 | | Observed Gain | 0 | | Observed Loss | 2 | | Observed Complex | 0 | | Frequency | n/a |
|
|