| Internal ID | 15558521 |
| Landmark | |
| Location Information | |
| Cytoband | 1q44 |
| Allele length | | Assembly | Allele length | | hg38 | 951 | | hg19 | 951 | | hg18 | 951 | | hg17 | 951 |
|
| Variant Type | CNV loss |
| Copy Number | |
| Allele State | |
| Allele Origin | |
| Probe Count | |
| Validation Flag | |
| Merged Status | M |
| Merged Variants | |
| Supporting Variants | nssv548059, nssv548058 |
| Samples | YH, JDW |
| Known Genes | OR2T11 |
| Method | Sequencing |
| Analysis | Using absolute estimates of copy number, we calculated an in silico log2 ratio for each of the three genome-wide comparisons and compared it with the experimental values determined by array CGH. |
| Platform | Illumina Genome Analyzer and Roche/454 sequencer. For arrayCGH validation experiments we used Nimblegen |
| Comments | OR2T11 |
| Reference | Alkan_et_al_2009 |
| Pubmed ID | 19718026 |
| Accession Number(s) | nsv471355
|
| Frequency | | Sample Size | 3 | | Observed Gain | 0 | | Observed Loss | 2 | | Observed Complex | 0 | | Frequency | n/a |
|
