Variant DetailsVariant: esv2661116Internal ID | 9580535 | Landmark | | Location Information | | Cytoband | 6q26 | Allele length | Assembly | Allele length | hg38 | 44757 | hg19 | 44757 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv5980908, essv6359179, essv6559307, essv6322106, essv6463000 | Samples | NA19355, NA19448, NA19383, NA19462, NA19375 | Known Genes | PARK2 | Method | Merging | Analysis | No reference, merging analysis | Platform | Merging | Comments | High quality site | Reference | 1000_Genomes_Consortium_Phase_1 | Pubmed ID | 23128226 | Accession Number(s) | esv2661116
| Frequency | Sample Size | 1151 | Observed Gain | 0 | Observed Loss | 5 | Observed Complex | 0 | Frequency | n/a |
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