| Internal ID | 22825835 |
| Landmark | |
| Location Information | |
| Cytoband | Xp11.21 |
| Allele length | | Assembly | Allele length | | hg38 | 15100 | | hg19 | 15100 |
|
| Variant Type | CNV deletion |
| Copy Number | |
| Allele State | |
| Allele Origin | |
| Probe Count | |
| Validation Flag | |
| Merged Status | M |
| Merged Variants | |
| Supporting Variants | nsv3195398, nsv3207033 |
| Samples | HG00512, NA19238, NA19239, HG00731, NA19240, HG00733 |
| Known Genes | |
| Method | Optical mapping
Sequencing |
| Analysis | BioNano Genomics proprietary analysis
Multiple analysis algorthms |
| Platform | BioNano Genomics
Illumina HiSeq |
| Comments | |
| Reference | Chaisson_et_al_2019 |
| Pubmed ID | 30992455 |
| Accession Number(s) | dgv10132n152
|
| Frequency | | Sample Size | 9 | | Observed Gain | 0 | | Observed Loss | 6 | | Observed Complex | 0 | | Frequency | n/a |
|
