Variant DetailsVariant: nssv618772Internal ID | 15471890 | Landmark | | Location Information | | Cytoband | 11q14.2 | Allele length | Assembly | Allele length | hg38 | 59143 | hg19 | 59143 | hg18 | 59143 | hg17 | 59143 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | S | Merged Variants | nsv508643 | Supporting Variants | | Samples | NA10860 | Known Genes | C11orf73, EED, MIR6755 | 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) | nssv618772
| Frequency | Sample Size | 4 | Observed Gain | 0 | Observed Loss | 1 | Observed Complex | 0 | Frequency | n/a |
|
|