Oncoplot of the most frequent genetic aberrations in the entire cohort (N = 132). Each column represents a unique patient. The top row represents both the number and type of alterations detected in each biopsy. Each row represents the diagnosis, biopsy, sequencing panel, gene and type of mutation, and/or CNA. Gray tiles indicate wild type. Missing tiles represent a gene that is not included in that specific NGS panel. Percent frequencies in the far-right column represent both mutations and CNAs for that specific gene.