Variant DetailsVariant: nssv7695Internal ID | 15189483 | Landmark | | Location Information | | Cytoband | 1q22 | Allele length | Assembly | Allele length | hg38 | 44757 | hg19 | 44757 | hg18 | 44757 | hg17 | 44757 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | S | Merged Variants | nsv3065 | Supporting Variants | | Samples | NA12156 | Known Genes | DAP3, GON4L, MSTO2P | Method | Sequencing | Analysis | End-sequence pairs were mapped to the human genome assembly (hg17) using a previously described algorithm (Tuzun et al 2005) | Platform | Capillary | Comments | | Reference | Kidd_et_al_2008 | Pubmed ID | 18451855 | Accession Number(s) | nssv7695
| Frequency | Sample Size | 9 | Observed Gain | 0 | Observed Loss | 1 | Observed Complex | 0 | Frequency | n/a |
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