Variant DetailsVariant: esv3621780Internal ID | 6661956 | Landmark | | Location Information | | Cytoband | 9q33.3 | Allele length | Assembly | Allele length | hg38 | 579 | hg19 | 579 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv13621953, essv13621948, essv13621954, essv13621945, essv13621949, essv13621950, essv13621952, essv13621947, essv13621951, essv13621946 | Samples | NA21115, HG04100, NA20884, HG03900, NA20875, HG02657, HG03940, HG03702, NA21125, HG03729 | Known Genes | GARNL3 | Method | Sequencing | Analysis | | Platform | Multiple platforms | Comments | | Reference | 1000_Genomes_Consortium_Phase_3 | Pubmed ID | 21293372 | Accession Number(s) | esv3621780
| Frequency | Sample Size | 2504 | Observed Gain | 0 | Observed Loss | 10 | Observed Complex | 0 | Frequency | n/a |
|
|