| Internal ID | 8505216 |
| Landmark | |
| Location Information | |
| Cytoband | 11p13 |
| Allele length | | Assembly | Allele length | | hg38 | 1338 | | hg19 | 1338 | | hg18 | 1338 |
|
| Variant Type | CNV deletion |
| Copy Number | |
| Allele State | |
| Allele Origin | |
| Probe Count | |
| Validation Flag | |
| Merged Status | M |
| Merged Variants | |
| Supporting Variants | essv5389173 |
| Samples | NA18507 |
| Known Genes | |
| Method | Sequencing |
| Analysis | Larger insertions and deletions are found by looking at variation in mate pair distances in the 2x50 mate pair libraries. These data are included in separate files for each of three coverage values: 2.2x, 4.0x, 5.6x, and 8.4x |
| Platform | Not specified |
| Comments | originalFile=Yoruban_large_indels_8.4x.gff |
| Reference | McKernan_et_al_2009 |
| Pubmed ID | 19546169 |
| Accession Number(s) | esv2441658
|
| Frequency | | Sample Size | 1 | | Observed Gain | 0 | | Observed Loss | 1 | | Observed Complex | 0 | | Frequency | n/a |
|
