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Variant allele fractions of SNVs of genes included in the targeted sequencing panel. In 15 cases with informative SNV analysis in the primary tumor and CSF cfDNA, the mutated allele fractions of SNVs in the tumor sample (x-axis) and in the CSF cfDNA (y-axis) are indicated. Pearson test showed a significant correlation (r = 0.51, p = 1.6 × 10−7).
