Common copy number polymorphism Results

[Jingjiao-ma]

Hi,

I called CNV using GenomeSTRiP software, I analyzed the CNV data via plink(v1.07) --gfile command,
and in the only results plink.gvar.summary FIELD and VALUE columns , what is the meaning of CNV yes or no?

What to do to get other information like the P and OR value from Basic case/control association test ？

Thank you
Best