Variant DetailsVariant: esv3623073Internal ID | 6663241 | Landmark | | Location Information | | Cytoband | 10q11.21 | Allele length | Assembly | Allele length | hg38 | 829 | hg19 | 829 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv13765106, essv13765110, essv13765107, essv13765102, essv13765116, essv13765108, essv13765113, essv13765101, essv13765115, essv13765104, essv13765117, essv13765112, essv13765103, essv13765111, essv13765109, essv13765114, essv13765105, essv13765100 | Samples | HG02583, NA19909, HG03280, HG02476, HG03074, HG03464, HG03209, HG02885, HG02820, NA19184, HG02511, HG03081, HG02878, HG01101, HG03064, NA06986, HG03039, NA18505 | Known Genes | TMEM72-AS1 | Method | Sequencing | Analysis | | Platform | Multiple platforms | Comments | | Reference | 1000_Genomes_Consortium_Phase_3 | Pubmed ID | 21293372 | Accession Number(s) | esv3623073
| Frequency | Sample Size | 2504 | Observed Gain | 0 | Observed Loss | 18 | Observed Complex | 0 | Frequency | n/a |
|
|