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[Preprint]. 2023 Mar 16:rs.3.rs-2675436. [Version 1] doi: 10.21203/rs.3.rs-2675436/v1

Figure 2. Specimens and molecular assays used in the current study.

Figure 2

Whole exome or whole genome sequencing germline variant calls were made using DNA obtained from 61 patients with available DNA from peripheral blood (n=11 SJCRH and n=50 COG). Paired tumor sets are samples from both right and left tumors in a patient with synchronous BWT (n=30). Unpaired tumors are samples from either the right or left tumor in a patient with synchronous BWT, but for whom one side was not available for analysis (n=37). Adjacent non-diseased kidney was confirmed by a pathologist and came from patients with tumors in the study. R – right L – left.