| Internal ID | 10162647 |
| Landmark | |
| Location Information | |
| Cytoband | 3p22.2 |
| Allele length | | Assembly | Allele length | | hg38 | 1100 | | hg19 | 1100 |
|
| Variant Type | CNV deletion |
| Copy Number | |
| Allele State | |
| Allele Origin | |
| Probe Count | |
| Validation Flag | |
| Merged Status | S |
| Merged Variants | esv2725165 |
| Supporting Variants | |
| Samples | SSM058 |
| Known Genes | SCN11A |
| Method | Sequencing |
| Analysis | Breakdancer:4 times standard deviation,VariationHunter:4 times standard deviation and at least 3 supportting reads |
| Platform | Illumina HiSeq 2000 |
| Comments | |
| Reference | Wong_et_al_2012b |
| Pubmed ID | 23290073 |
| Accession Number(s) | essv6753928
|
| Frequency | | Sample Size | 96 | | Observed Gain | 0 | | Observed Loss | 1 | | Observed Complex | 0 | | Frequency | n/a |
|
