Variant DetailsVariant: esv3587622Internal ID | 6627923 | Landmark | | Location Information | | Cytoband | 1q22 | Allele length | Assembly | Allele length | hg38 | 23185 | hg19 | 23185 |
| Variant Type | CNV gain | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | dgv55e214 | Supporting Variants | essv10152246, essv10152243, essv10152240, essv10152245, essv10152257, essv10152236, essv10152221, essv10152220, essv10152230, essv10152256, essv10152241, essv10152234, essv10152237, essv10152222, essv10152252, essv10152224, essv10152244, essv10152259, essv10152247, essv10152251, essv10152254, essv10152258, essv10152219, essv10152228, essv10152223, essv10152229, essv10152227, essv10152242, essv10152238, essv10152253, essv10152232, essv10152248, essv10152235, essv10152231, essv10152239, essv10152250, essv10152226, essv10152225, essv10152255, essv10152249, essv10152233 | Samples | NA20339, HG02628, NA19909, NA19332, NA18877, NA18878, HG03126, HG03193, HG03577, NA18510, NA19107, NA19171, HG03436, HG01393, NA19130, NA19917, NA18864, NA19908, HG03132, HG03547, HG01882, HG02887, HG02307, HG03575, HG01889, HG03563, NA19461, HG02445, HG02309, NA19318, HG03109, NA19436, HG02455, NA19834, NA19334, HG02982, NA19323, HG01912, NA19468, NA19102, HG02284 | Known Genes | GBA, GBAP1, MTX1 | Method | Sequencing | Analysis | | Platform | Multiple platforms | Comments | | Reference | 1000_Genomes_Consortium_Phase_3 | Pubmed ID | 21293372 | Accession Number(s) | esv3587622
| Frequency | Sample Size | 2504 | Observed Gain | 41 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
|
|