Variant DetailsVariant: esv2658845Internal ID | 9578264 | Landmark | | Location Information | | Cytoband | 9q34.11 | Allele length | Assembly | Allele length | hg38 | 5048 | hg19 | 5048 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | dgv1380e199 | Supporting Variants | essv6192724, essv5465933, essv5605760, essv6394940, essv6306856, essv5436089, essv5902289, essv5610468, essv5960440, essv5799245, essv5499725, essv5521686, essv5558273 | Samples | NA19466, NA19374, NA19373, NA19315, NA19437, NA19327, NA19338, NA19469, NA19470, NA19311, NA19438, NA19346, NA19431 | Known Genes | | Method | Merging | Analysis | No reference, merging analysis | Platform | Merging | Comments | | Reference | 1000_Genomes_Consortium_Phase_1 | Pubmed ID | 23128226 | Accession Number(s) | esv2658845
| Frequency | Sample Size | 1151 | Observed Gain | 0 | Observed Loss | 13 | Observed Complex | 0 | Frequency | n/a |
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