| Internal ID | 15546668 |
| Landmark | |
| Location Information | |
| Cytoband | 17q22 |
| Allele length | | Assembly | Allele length | | hg38 | 46750 | | hg19 | 46750 | | hg18 | 46750 | | hg17 | 46750 |
|
| Variant Type | CNV deletion |
| Copy Number | |
| Allele State | |
| Allele Origin | |
| Probe Count | |
| Validation Flag | |
| Merged Status | M |
| Merged Variants | |
| Supporting Variants | nssv1380 |
| Samples | NA19240 |
| Known Genes | RNF126P1 |
| 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) | nsv2105
|
| Frequency | | Sample Size | 9 | | Observed Gain | 0 | | Observed Loss | 1 | | Observed Complex | 0 | | Frequency | n/a |
|
