Variant DetailsVariant: esv3623051Internal ID | 6663219 | Landmark | | Location Information | | Cytoband | 10q11.21 | Allele length | Assembly | Allele length | hg38 | 743 | hg19 | 743 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv13764540, essv13764535, essv13764544, essv13764538, essv13764550, essv13764545, essv13764534, essv13764543, essv13764541, essv13764547, essv13764542, essv13764537, essv13764549, essv13764536, essv13764548, essv13764546, essv13764533, essv13764539, essv13764531, essv13764532 | Samples | HG01359, HG02476, NA19355, HG03139, NA18870, NA19201, HG02549, HG02860, NA19383, NA18874, NA19239, HG01626, HG02439, HG02322, HG01889, HG02555, NA18856, HG01697, HG03117, NA06986 | Known Genes | LINC00840 | Method | Sequencing | Analysis | | Platform | Multiple platforms | Comments | | Reference | 1000_Genomes_Consortium_Phase_3 | Pubmed ID | 21293372 | Accession Number(s) | esv3623051
| Frequency | Sample Size | 2504 | Observed Gain | 0 | Observed Loss | 20 | Observed Complex | 0 | Frequency | n/a |
|
|