Variant DetailsVariant: nsv7306Internal ID | 15205616 | Landmark | | Location Information | | Cytoband | 19p12 | Allele length | Assembly | Allele length | hg38 | 485161 | hg19 | 485161 | hg18 | 485161 | hg17 | 485161 |
| Variant Type | OTHER inversion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv10179, nssv10178 | Samples | NA18956 | Known Genes | LOC641367, ZNF100, ZNF208, ZNF257, ZNF43 | 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) | nsv7306
| Frequency | Sample Size | 9 | Observed Gain | 0 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
|
|