Recurrent genomic MCL alterations identified using WGS/WES analysis. The frequencies displayed correspond to the studies detailed in Table 1. (A) Illustrates the CNA observed (overall frequency ≥2%) in 202 patients with MCL. The frequency of genomic alterations highlighted with an asterisk “∗” is based only on the Nadeu et al⁵ publication. (B) CNA identified in Nadeu et al⁵ categorized by MCL subtype. (C) Single nucleotide variants (SNVs) and insertions and deletions (indels) with overall frequency ≥2%, identified in 432 patients with MCL. (D) SNVs and indels, identified in Nadeu et al⁵ and categorized by MCL subtype. Variants with an overall frequency ≥2% in at least 1 of the MCL subtypes are displayed.