Variant DetailsVariant: esv2669542Internal ID | 9588961 | Landmark | | Location Information | | Cytoband | 6q26 | Allele length | Assembly | Allele length | hg38 | 4098 | hg19 | 4098 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | dgv1167e199 | Supporting Variants | essv6589118, essv6570749, essv5607151, essv5817543, essv5458601, essv6493955, essv5951920, essv5498903, essv5862024 | Samples | NA19648, NA19678, NA19771, NA19782, NA19720, NA19749, NA19747, NA19661, NA19755 | Known Genes | PARK2 | Method | Merging | Analysis | No reference, merging analysis | Platform | Merging | Comments | | Reference | 1000_Genomes_Consortium_Phase_1 | Pubmed ID | 23128226 | Accession Number(s) | esv2669542
| Frequency | Sample Size | 1151 | Observed Gain | 0 | Observed Loss | 9 | Observed Complex | 0 | Frequency | n/a |
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