Variant DetailsVariant: esv3611497Internal ID | 6651715 | Landmark | | Location Information | | Cytoband | 6q26 | Allele length | Assembly | Allele length | hg38 | 11942 | hg19 | 11942 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | dgv1233e214 | Supporting Variants | essv12620693, essv12620694, essv12620696, essv12620697, essv12620695, essv12620698 | Samples | NA19703, HG03717, HG00182, HG03740, NA19059, HG00372 | Known Genes | PARK2 | Method | Sequencing | Analysis | | Platform | Multiple platforms | Comments | | Reference | 1000_Genomes_Consortium_Phase_3 | Pubmed ID | 21293372 | Accession Number(s) | esv3611497
| Frequency | Sample Size | 2504 | Observed Gain | 0 | Observed Loss | 6 | Observed Complex | 0 | Frequency | n/a |
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