One of the main use cases for the Progenetix resource is the exploration of frequency and disease specificity of genes of interest. Traditionally, the relevance of somatic CNVs hitting a gene in the context of cancer are judged by
The Progenetix Search Page supports the exploration of regional CNVs through
The response of the queries for genomic variants provide some basic statistics, e.g. the relative frequencies of these variants for each classification code (e.g. NCIT, ICD-O) encountered in teh matched samples.