Pathogenicity and functional impact of non-frameshifting insertion/deletion variation in the human genome
Fig 6
Histogram of predicted pathogenicity scores for (A) the training data using cross-validation, (B) cancer driver mutations from dbCID (yellow), highly recurrent variants (COSMIC-R, red) compared to the background in COSMIC (blue), (C) de novo non-frameshifting insertion/deletion variants in individuals with autism spectrum disorder (ASD, red) and de novo variation from unaffected siblings (Control, blue).