Yes, I was tested for CMV as well, and came back totally negative - I've never had it at all, which did worry me slightly as I work with small children so I am at risk of catching it! I'm using lots of hand sanitiser at the moment!
Both you and your partner have to be carriers of the gene for your baby to be at risk of having CF. However, the CF test only looks for the most common gene mutations - there are a few less common mutations that it can't check for, but they are so uncommon that it is unlikely that you would have them. Did your consultant not explain that?
And yep, my partner got tested as well, and his results were also negative.
My consultant thought that the bowel had shown up as echogenic because I am fairly slim (well, I am when not pregnant!!!) - she thought the normal ultrasound settings might just have been too high for me.
So have you got another week to wait? Please try not to worry - even in the unlikely scenario that both you and your partner had the recessive CF gene, there's only, I think, a 25% chance that your baby would then have CF. And if your baby's bowel is looking less white now then I'm sure that must be a good sign? Fingers crossed for you and your baby.