NOTCH2NLC and neuronal intranuclear inclusion disease: For example, the intronic repeat in NOP56, which causes spinocerebellar ataxia 36, had an average of 20× coverage, depending on the capture kit; repeats in UTRs, such as JPH3, DMPK, NOTCH2NLC and PPP2R2B (which cause Huntington disease-like 2, myotonic dystrophy type 1, neuronal intranuclear inclusion disease and spinocerebellar ataxia 12), were also captured and their genotypes predicted (Figure 5, Supplementary Table S2).