| | NEGR1 deletion | BTNL8-BTNL3 deletion |
|---|
| Calgary Cohort (n = 8) | 100% | 62.5% |
| CBTTC (n = 73) | 86.3% | 17.8% |
| MSSNG controls (n = 2596) | 87.1% | 48.0% |
| 1000 Genomes Project (n = 2504) | 89% | 38.2% |
| Personal Genome Project Canada (n = 93) | 77.4% | 48.4% |
- Datasets include the Calgary cohort, a pediatric HGG dataset from the CBTTC and individuals from the general population (coded parental control Canadian samples in MSSNG); 1000 Genomes Project CNVs obtained from the Database of Genomic Variants [DGV]; and control samples from Personal Genome Project Canada (PGPC)). Deletions are either heterozygous or homozygous
