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Genetic alterations of SLC38s family in integrated ESCC cohort. Somatic mutations of SLC38s family were analyzed in 490 paired ESCC samples and CNAs were analyzed in 314 paired ESCC samples. (A) Genomic landscape of SLC38s family; (B) Scatter plot showed relative copy number variations of SLC38s family. SLC38s, solute carrier family 38; ESCC, esophageal squamous cell carcinoma; CNA, copy number alteration.
