| Internal ID | 18273756 |
| Landmark | |
| Location Information | |
| Cytoband | 12p13.33 |
| Allele length | | Assembly | Allele length | | hg38 | 190133 | | hg19 | 197967 | | hg18 | 197967 |
|
| Variant Type | CNV gain |
| Copy Number | |
| Allele State | |
| Allele Origin | |
| Probe Count | |
| Validation Flag | |
| Merged Status | S |
| Merged Variants | nsv428269 |
| Supporting Variants | |
| Samples | HGDP00476 |
| Known Genes | FAM138D, IQSEC3, LOC574538, SLC6A12, SLC6A13 |
| Method | BAC aCGH |
| Analysis | Copy number variable segments were automatically detected using the CNVfinder algorithm (Fiegler et al. 2006). |
| Platform | Sanger H. sapiens Whole Genome Tile Path 28.7k v3 |
| Comments | |
| Reference | Perry_et_al_2008b |
| Pubmed ID | 18775914 |
| Accession Number(s) | nssv452238
|
| Frequency | | Sample Size | 62 | | Observed Gain | 1 | | Observed Loss | 0 | | Observed Complex | 0 | | Frequency | n/a |
|
