| Internal ID | 15478161 |
| Landmark | |
| Location Information | |
| Cytoband | 15q23 |
| Allele length | | Assembly | Allele length | | hg38 | 32687 | | hg19 | 32687 | | hg18 | 32687 | | hg17 | 32687 |
|
| Variant Type | CNV deletion |
| Copy Number | |
| Allele State | |
| Allele Origin | |
| Probe Count | |
| Validation Flag | |
| Merged Status | M |
| Merged Variants | |
| Supporting Variants | nssv617422 |
| Samples | CHM |
| Known Genes | MYO9A, SENP8 |
| Method | Optical mapping |
| Analysis | Single-molecule optical maps were assembled into genome-wide consensus maps. These consensus maps were compared to a restriction map generated from the NCBI b35 human genome reference sequence. |
| Platform | Optical Mapping |
| Comments | |
| Reference | Teague_et_al_2010 |
| Pubmed ID | 20534489 |
| Accession Number(s) | nsv510665
|
| Frequency | | Sample Size | 4 | | Observed Gain | 0 | | Observed Loss | 1 | | Observed Complex | 0 | | Frequency | n/a |
|
