Variant DetailsVariant: esv2674153Internal ID | 9593572 | Landmark | | Location Information | | Cytoband | 7q21.13 | Allele length | Assembly | Allele length | hg38 | 1039 | hg19 | 1039 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv6359370, essv6566981, essv5561496, essv6464245, essv6280844 | Samples | NA19457, NA18908, NA19469, NA18517, NA19324 | Known Genes | ZNF804B | 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) | esv2674153
| Frequency | Sample Size | 1151 | Observed Gain | 0 | Observed Loss | 5 | Observed Complex | 0 | Frequency | n/a |
|
|