Variant DetailsVariant: essv7504871Internal ID | 10436467 | Landmark | | Location Information | | Cytoband | 22q12.3 | Allele length | Assembly | Allele length | hg38 | 152 | hg19 | 152 |
| Variant Type | CNV deletion | Copy Number | | Allele State | Homozygous | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | S | Merged Variants | esv3235304 | Supporting Variants | | Samples | HuRef | Known Genes | LARGE | Method | Sequencing | Analysis | | Platform | Complete Genomics | Comments | | Reference | Pang_et_al_2013b | Pubmed ID | 24192839 | Accession Number(s) | essv7504871
| Frequency | Sample Size | 1 | Observed Gain | 0 | Observed Loss | 1 | Observed Complex | 0 | Frequency | n/a |
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