Variant DetailsVariant: esv2662571Internal ID | 9581990 | Landmark | | Location Information | | Cytoband | 9q34.11 | Allele length | Assembly | Allele length | hg38 | 4088 | hg19 | 4088 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | dgv1380e199 | Supporting Variants | essv5439177, essv5602454, essv5549588, essv6314888, essv5874639, essv5502330, essv5945592, essv6099102, essv6123575, essv6283585, essv6233151, essv6046725, essv6122077, essv6228461 | Samples | NA19466, NA19315, NA19138, NA18908, NA18910, NA19469, NA19834, NA19712, NA19470, NA19311, HG01108, NA20281, NA19438, NA19129 | Known Genes | | 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) | esv2662571
| Frequency | Sample Size | 1151 | Observed Gain | 0 | Observed Loss | 14 | Observed Complex | 0 | Frequency | n/a |
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