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    • #15895
      genetherapy
      Participant

      Hi all,
      I really in trouble with CNV databases? I need this information for my presentation,I never study Copy Number Variation before. I find a programme at Sanger Institute but the software support linux and MAC so I can’t use it. Is there any CNV databases where I can detect CNVs?
      I will appreciate if someone help me 🙄

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