Variant DetailsVariant: esv3622098 Internal ID | 6662268 | Landmark | | Location Information | | Cytoband | 10p15.3 | Allele length | Assembly | Allele length | hg38 | 1410 | hg19 | 1410 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv13664681, essv13664689, essv13664683, essv13664704, essv13664703, essv13664680, essv13664694, essv13664701, essv13664677, essv13664702, essv13664682, essv13664708, essv13664686, essv13664709, essv13664676, essv13664684, essv13664678, essv13664700, essv13664698, essv13664687, essv13664691, essv13664707, essv13664699, essv13664690, essv13664706, essv13664695, essv13664685, essv13664697, essv13664688, essv13664692, essv13664693, essv13664696, essv13664705, essv13664679 | Samples | HG02944, HG02419, HG02836, HG02891, NA19350, HG03100, NA19307, HG02922, HG03268, NA18868, NA19385, HG02571, HG02623, HG03055, NA19921, HG03169, HG03124, HG03382, HG03046, HG02568, NA19017, NA19401, HG03028, NA19435, NA20351, NA18865, NA19143, HG02938, HG03060, NA19116, HG03470, HG02643, NA19431, HG01747 | Known Genes | ADARB2 | Method | Sequencing | Analysis | | Platform | Multiple platforms | Comments | | Reference | 1000_Genomes_Consortium_Phase_3 | Pubmed ID | 21293372 | Accession Number(s) | esv3622098
| Frequency | Sample Size | 2504 | Observed Gain | 0 | Observed Loss | 34 | Observed Complex | 0 | Frequency | n/a |
|
|