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Fig. 2 | BMC Cancer

Fig. 2

From: Real-world application of targeted next-generation sequencing for identifying molecular variants in Asian non-small-cell lung cancer

Fig. 2

Distribution of clinically relevant variants in NSCLC patients. A Proportion of NSCLC samples with different types of genetic alterations, including single nucleotide variants (SNVs) and insertions and deletions (Indels), copy number variations (CNVs), MET exon skipping alterations, and gene fusions. B Prevalence of actionable driver mutations in NSCLC

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BMC Cancer

ISSN: 1471-2407

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