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hello my name is erica anderson and today ill be discussing resources used for clinical copy number variant or cnv interpretation ill review new metrics and reporting recommendations developed by our cnv interpretation guidelines committee as well as details on how to use our publicly available dosage sensitivity map resources relating to cnv interpretation are available on the conference website and will be covered in more detail during this workshop id like to start by highlighting a couple of challenges to the cnv interpretation process the first being that most cnbs are unique or non-recurrent and thus have variable break points in gene content this figure shows some examples of unique cnvs involving many genes few genes and no genes during clinical encounter evaluating each of these cnvs will involve compiling evidence from different resources then using standardized processes to classify each appropriately followed by tailoring the clinical report for any cnvs that meet your l
