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Incidence of Molecular Subtypes within Our Cohort
| Molecular Type | Total | Caucasian | Mixed | Non-Caucasian |
|---|---|---|---|---|
| % | % | % | % | |
| IC1 GOM1 | 10.8% | 9.7% | 12.5% | 13.6% |
| IC2 LOM2 | 48.2% | 51.6% | 50.0% | 31.8% |
| pUPD113 | 29.5% | 25.8% | 29.2% | 45.5% |
| CDKN1C mutation | 3.6% | 4.3% | 4.2% | 0% |
| Chromosome 11p15 abnormality | 7.9% | 8.6% | 4.2% | 9.1% |
Imprinting center 1 gain of methylation
Imprinting center 2 loss of methylation
Paternal uniparental disomy of chromosome 11
