Everyone here descends (or presumably descends) from Hans Adam STRAUB (1666-1726) of Großgartach, Württemberg, and the test subjects average 10 to 12 generations from him. 

The individual highlighted in yellow (below) descends from Hans Adam's son, Antonius STRAUB, who remained in Germany, while everyone else in the table descends from Antonius's brother, Johann Pieter STRAUB, who immigrated to Philadelphia, PA, in 1733.

The first data column shows the individual's GD from the family's modal haplotype.  No one has a GD from this haplotype greater than three at 67 markers or four at 111 markers.

The most frequent GDs between family members with a common ancestor 10 or 11 generations back are 1 or 2 at 67 markers or 3 or 4 at 111 markers.

The other columns show the frequencies for the GDs each individual has from each of the other members of the family.  Not surprisingly, GD from the family's modal haplotype roughly correlates with GDs from each other.  No one has a GD from anyone else greater than five at 67 markers or eight at 111 markers.

Every tested descendant tells you something, not to mention that every male needs to be tested, if for no other reason, than to establish that he does not have an NPE in his patrilineal line.  The empirical NPE rate in my projects is running at least 10%, so it is not a possibility to simply dismiss — no matter how solidly documented your paper genealogy is, you still could have an NPE.  By definition, an NPE is unexpected.