On the other hand, LI1, RASSF2, IL3RA, FGD2, IRF8, GIMAP4, GIMAP6, ITGA5, TGM2, RAMP2, CSF2RB, ARHGAP29, PALMD, MMRN2, and STC1 exhibited a higher frequency of missing CNVs for deletions, suggesting potential tumor suppressor roles for these genes (Fig. 3D). The gene discussed is STC1; the disease is neoplasm.